| Literature DB >> 26500339 |
María-Victoria Mateos1, Joaquín Martínez-López2, Miguel-Teodoro Hernández3, Enrique-M Ocio1, Laura Rosiñol4, Rafael Martínez5, Ana-Isabel Teruel6, Norma C Gutiérrez1, María-Luisa Martín Ramos2, Albert Oriol7, Joan Bargay8, Enrique Bengoechea9, Yolanda González10, Jaime Pérez de Oteyza11, Mercedes Gironella12, Cristina Encinas13, Jesús Martín14, Carmen Cabrera15, Bruno Paiva16, María-Teresa Cedena2, Noemí Puig1, Joan Bladé4, Juan-José Lahuerta2, Jesús San-Miguel16.
Abstract
Bortezomib plus melphalan and prednisone (VMP) and lenalidomide plus low-dose dexamethasone (Rd) are 2 standards of care for elderly untreated multiple myeloma (MM) patients. We planned to use VMP and Rd for 18 cycles in a sequential or alternating scheme. Patients (233) with untreated MM, >65 years, were randomized to receive 9 cycles of VMP followed by 9 cycles of Rd (sequential scheme; n = 118) vs 1 cycle of VMP followed by 1 cycle of Rd, and so on, up to 18 cycles (alternating scheme; n = 115). VMP consisted of one 6-week cycle of bortezomib using a biweekly schedule, followed by eight 5-week cycles of once-weekly VMP. Rd included nine 4-week cycles of Rd. The primary end points were 18-month progression free survival (PFS) and safety profile of both schemes. The 18-month PFS was 74% and 80% in the sequential and alternating arms, respectively (P = .21). The sequential and alternating groups exhibited similar hematologic and nonhematologic toxicity. Both arms yielded similar complete response rate (42% and 40%), median PFS (32 months vs 34 months, P = .65), and 3-year overall survival (72% vs 74%, P = .63). The benefit of both schemes was remarkable in patients aged 65 to 75 years. In addition, achieving complete and immunophenotypic response was associated with better outcome. The present approach, based on VMP and Rd, is associated with high efficacy and acceptable toxicity profile with no differences between the sequential and alternating regimens. This trial was registered at www.clinicaltrials.gov as #NCT00443235.Entities:
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Year: 2015 PMID: 26500339 DOI: 10.1182/blood-2015-08-666537
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113